Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Polybasic nitrogen heterocyclic non-natural chiral amino acid and synthesis method thereof

A technology of chiral amino acid and synthesis method, which is applied in the field of chiral drug synthesis, can solve the problems of high synthesis cost, complex process, and low ee value, and achieve the effect of various types, simple process, and mature process

Active Publication Date: 2018-11-06
广西茵诺圣药业有限公司
View PDF7 Cites 5 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0009] Aiming at the problems existing in the prior art, the present invention provides a series of multivariate nitrogen-heterocyclic non-natural chiral amino acids and a synthesis method thereof to solve the problem of high synthesis cost and complicated process of existing nitrogen-heterocyclic non-natural chiral amino acids, ee worthless technical issues

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Polybasic nitrogen heterocyclic non-natural chiral amino acid and synthesis method thereof
  • Polybasic nitrogen heterocyclic non-natural chiral amino acid and synthesis method thereof
  • Polybasic nitrogen heterocyclic non-natural chiral amino acid and synthesis method thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0062] Example 1 fully embodies the synthesis process of (S)-ethyleneimino-2-carboxylic acid and (R)-ethyleneimino-2-carboxylic acid.

[0063] Example 1:

[0064] (1), the synthesis of 2-Boc-diethyl aminomalonate

[0065]

[0066] Compound 1 (450g, 2.13mol) was dissolved in 1L of dichloromethane, and triethylamine (646g, 6.39mol) was added dropwise in an ice-water bath, and the dropwise reaction was completed at room temperature for 0.5h; under cooling in an ice-water bath, Boc was slowly added dropwise Acid anhydride (512 g, 2.34 mol) was added dropwise and stirred overnight at room temperature. TLC showed that compound 1 disappeared, the reaction solution was filtered, the filter cake was washed with dichloromethane, and the filtrate was concentrated to obtain an oil. The oil was dissolved in ethyl acetate, washed with 1N hydrochloric acid aqueous solution, and then washed with saturated brine, the organic phase was dried over anhydrous sodium sulfate, filtered, and t...

Embodiment 2

[0092] Example 2 fully embodies the synthesis process of (S)-cycloheximino-2-carboxylic acid and (R)-cycloheximino-2-carboxylic acid.

[0093] Example 2:

[0094] (1), the synthesis of 2-Boc-diethyl aminomalonate

[0095]

[0096] Compound 1 (450g, 2.13mol) was dissolved in 1L of dichloromethane, and triethylamine (646g, 6.39mol) was added dropwise in an ice-water bath, and the dropwise reaction was completed at room temperature for 0.5h; under cooling in an ice-water bath, Boc was slowly added dropwise Acid anhydride (512 g, 2.34 mol) was added dropwise and stirred overnight at room temperature. TLC showed that compound 1 disappeared, the reaction solution was filtered, the filter cake was washed with dichloromethane, and the filtrate was concentrated to obtain an oil. The oil was dissolved in ethyl acetate, washed with 1N hydrochloric acid aqueous solution, and then washed with saturated brine, the organic phase was dried over anhydrous sodium sulfate, filtered, and t...

Embodiment 3

[0122] Example 3 fully embodies the synthesis process of (S)-cycloundecimino-2-carboxylic acid and (R)-cycloundecimino-2-carboxylic acid.

[0123] Example 3:

[0124] (1), the synthesis of 2-Boc-diethyl aminomalonate

[0125]

[0126] Compound 1 (500g, 2.36mol) was dissolved in 1L of dichloromethane, and triethylamine (716g, 7.08mol) was added dropwise in an ice-water bath. Acid anhydride (567g, 2.60mol) was added dropwise and stirred at room temperature overnight. TLC showed that compound 1 disappeared, the reaction solution was filtered, the filter cake was washed with dichloromethane, and the filtrate was concentrated to obtain an oil. The oil was dissolved in ethyl acetate, washed with 1N hydrochloric acid aqueous solution, and then washed with saturated brine, the organic phase was dried over anhydrous sodium sulfate, filtered, and the organic phase was concentrated to obtain 578 g of yellow oil compound 2 (yield: 89%). The next reaction was carried out directly w...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

No PUM Login to View More

Abstract

The invention relates to a polybasic nitrogen heterocyclic non-natural chiral amino acid and a synthesis method thereof. The amino acid can be applied to molecule building for antibiotic synthesis. According to the synthesis method, 2-aminodiethyl malonate and halogenated alkanes carry out substitution reactions, cyclization reactions, and decarboxylation reactions, and the reaction products are split to obtain the polybasic nitrogen heterocyclic non-natural chiral amino acid. The provided novel synthesis method has the advantages of simple synthesis route, low cost, convenient operation, andeasiness for commercial production, the chiral purity of obtained products is high, and the application prospect is good.

Description

technical field [0001] The invention relates to the field of chiral drug synthesis, in particular to the synthesis of a series of multivariate nitrogen-heterocyclic non-natural chiral amino acids. This type of non-natural amino acid is mainly used in drug synthesis and has a good application prospect in the field of drug synthesis. Background technique [0002] With the rapid development of chiral drug synthesis technology, higher requirements are put forward for the types and structures of chiral unnatural amino acids, and the emergence of some azachiral unnatural amino acids provides an opportunity for the design of new drugs. [0003] There are mainly the following two synthesis methods reported in the literature of chiral azapolycyclic unnatural amino acids, taking seven-membered rings as an example, but not limited to seven-membered rings: [0004] [0005] This is a chiral induction method using (1S,2R)-2-amino-1,2-diphenylethanol as a substrate (Journal of Medicina...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
Patent Type & Authority Applications(China)
IPC IPC(8): C07D203/08C07D223/06C07D225/02
CPCC07B2200/07C07D203/08C07D223/06C07D225/02Y02P20/55
Inventor 邱雪辉林文泉巫江钦杨保荣
Owner 广西茵诺圣药业有限公司
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com